Sathiyalingam, Shainthavaan and Roesner, Stefan (2022) Synthesis of α- and β-carbolines by a etalation/Negishi cross-coupling/SNAr reaction sequence. Advanced Synthesis & Catalysis, 364 (10). pp. 1769-1774. doi:10.1002/adsc.202200127

Dean, Conor, Roesner, Stefan, Rajkumar, Sundaram, Clarkson, Guy J., Jones, Matthew and Shipman, Michael (2021) Synthesis of sp3-rich chemical libraries based upon 1,2-Diazetidines. Tetrahedron, 79 . 131836. doi:10.1016/j.tet.2020.131836

Roesner, Stefan, Beadle, Jonathan D., Tam, Leo K. B., Wilkening, Ina, Clarkson, Guy J., Raubo, Piotr and Shipman, Michael (2020) Development of oxetane modified building blocks for peptide synthesis. Organic & Biomolecular Chemistry, 18 (28). pp. 5400-5405. doi:10.1039/D0OB01208D

Dean, Conor, Rajkumar, Sundaram, Roesner, Stefan, Carson, Nessa, Clarkson, Guy J., Wills, Martin, Jones, Matthew L. and Shipman, Michael (2020) Readily accessible sp3-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality. Chemical Science, 11 (6). pp. 1636-1642. doi:10.1039/C9SC04849A

Roesner, Stefan, Saunders, George J., Wilkening, Ina, Jayawant, Eleanor, Geden, Joanna V., Kerby, Paul D., Dixon, Ann M., Notman, Rebecca and Shipman, Michael (2019) Macrocyclisation of small peptides enabled by oxetane incorporation. Chemical Science, 10 (8). pp. 2465-2472. doi:10.1039/C8SC05474F

Noble, Adam, Roesner, Stefan and Aggarwal, Varinder K. (2016) Short enantioselective total synthesis of tatanan A and 3-epi-tatanan A using assembly-line synthesis. Angewandte Chemie International Edition, 55 (51). pp. 15920-15924. doi:10.1002/anie.201609598

Roesner, Stefan and Buchwald, Stephen L. (2016) Continuous-flow synthesis of biaryls by negishi cross-coupling of fluoro- and trifluoromethyl-substituted (hetero)arenes. Angewandte Chemie International Edition, 55 (35). pp. 10463-10467. doi:10.1002/anie.201605584

Roesner, Stefan, Blair, Daniel J. and Aggarwal, Varinder K. (2015) Enantioselective installation of adjacent tertiary benzylic stereocentres using lithiation–borylation–protodeboronation methodology. Application to the synthesis of bifluranol and fluorohexestrol. Chemical Science, 6 (7). pp. 3718-3723. doi:10.1039/C4SC03901G